甜菜碱
溶菌酶
尿素
变性(裂变材料)
渗透压
化学
分子
氢键
质子核磁共振
核磁共振波谱
结晶学
立体化学
有机化学
生物化学
核化学
作者
Jiantao Chen,Xiangjun Gong,Chaoxi Zeng,Yonghua Wang,Guangzhao Zhang
标识
DOI:10.1021/acs.jpcb.6b10172
摘要
It is known that urea can induce protein denaturation that can be inhibited by osmolytes. Yet, experimental explorations on this mechanism at the molecular level are still lacking. We have investigated the resistance of betaine to the urea-induced denaturation of lysozyme in aqueous solutions using low-field NMR. Our study demonstrates that urea molecules directly interact with lysozyme, leading to denaturation. However, betaine molecules interacting with urea more strongly than lysozyme can pull the bound urea molecules from lysozyme so that the protein is protected from denaturation. The number of urea molecules bound to a betaine molecule is given under different conditions. Proton NMR spectroscopy ( 1 H-NMR) and Fourier transform infrared spectroscopy reveal that the interaction between betaine and urea is through hydrogen bonding.
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